# FDA Inspection 756390 - Orthoip Llc dba FxDevices - November 30, 2011

Source: https://www.keypedia.com/records/fda_inspections/orthoip-llc-dba-fxdevices/e7b0617f-b540-4040-b43b-5f858c66c59e
Source feed: FDA_Inspections

> FDA Inspection 756390 for Orthoip Llc dba FxDevices on November 30, 2011. Classification: Voluntary Action Indicated (VAI).

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## Details

- Record Type: FDA Inspection
- Inspection ID: 756390
- Company Name: Orthoip Llc dba FxDevices
- Inspection Date: 2011-11-30
- Classification: Voluntary Action Indicated (VAI)
- Project Area: Postmarket Assurance: Devices
- Product Type: Devices
- Office Name: Center for Devices and Radiological Health

## Related Documents

- [FDA Inspection 756390 - 2011-11-30](https://www.keypedia.com/records/fda_inspections/orthoip-llc-dba-fxdevices/f12213aa-1695-40de-8995-add9f21d1130)

Company: https://www.keypedia.com/companies/orthoip-llc-dba-fxdevices/21201d7a-f904-4367-9673-186e53e0ee26

Office: https://www.keypedia.com/offices/center-for-devices-and-radiological-health/9d89aff6-e435-4764-87be-f58c01aca7f7